Angiodynamics recalls Soft-Vu Angiographic Catheters with a defect that may prevent guidewires from passing through the hub. Affected models include SOFT-VU SO1 4F X 80CM 038 NB 0SH. Consumers should contact the company for details.
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
Angiodynamics is recalling certain Soft-Vu Angiographic Catheters due to a manufacturing defect that may prevent the correct size guidewire from passing through the catheter hub. This could lead to complications during medical procedures if the catheter cannot be properly navigated.
The defect prevents the appropriately sized guidewire from passing through the inner diameter of the catheter hub. This could cause the catheter to become stuck during medical procedures, potentially leading to complications like bleeding or tissue damage.
Healthcare professionals using the catheter for medical procedures are most at risk. Patients receiving the catheter during procedures may also be affected if the defect causes complications.
Check for the model SOFT-VU SO1 4F X 80CM 038 NB 0SH with catalog number 10714024. The product comes in a box with 5 pouches and has specific lot numbers: A2825152 or A3225009.
Identify the model and lot numbers to confirm if your catheter is affected.
The recall states the catheter has a manufacturing defect that may prevent guidewires from passing through the hub, so it is not safe to use without verification.
Check for the model SOFT-VU SO1 4F X 80CM 038 NB 0SH with catalog number 10714024 and lot numbers A2825152 or A3225009.
Contact Angiodynamics for details on the remedy, as the recall record does not specify a remedy.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-1867-2026 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-1867-2026 from Angiodynamics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
